Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 12:25245284 (forward strand) | View in location tab

Co-located

with COSMIC COSM1168054 (G/T), COSM1360859 (G/A) ; HGMD-PUBLIC CM061081, CM070967, CM070968

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_081_KRAS_190070_0013, 5695

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and is associated with 5 phenotypes.

Variant displays